A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608974



Internal ID16049697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149188785..149237608hg38UCSC Ensembl
Innerchr7:148885877..148934699hg19UCSC Ensembl
Innerchr7:148516810..148565632hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3848824
hg1948823
hg1848823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11712n54
Supporting Variantsnssv1099467
Samples
Known GenesZNF282
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608974
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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